Allele/Variant

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Category 

Variant Type

Molecular Consequence

23 results
Allele/Variant Genes: Myf6 (Mmu) Molecular Consequence: intron variant
Allele/Variant
Source: rs30611318
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329401A>C

Allele/Variant
Source: rs584909182
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329536G>A

Allele/Variant
Source: rs8258515
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329783G>A

Allele/Variant
Source: rs579329232
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329529G>A

Allele/Variant
Source: rs584749265
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329519G>A

Allele/Variant
Source: rs8258514
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329861T>C

Allele/Variant
Source: rs8258513
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329946G>C

Allele/Variant
Source: rs30611316
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329373T>C

Allele/Variant
Source: rs16799522
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329497C>T

Allele/Variant
Source: rs257293555
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329395G>A

Allele/Variant
Source: rs8258516
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329631G>A

Allele/Variant
Source: rs261328925
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329947C>T

Allele/Variant
Source: rs225081571
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107330037A>C

Allele/Variant
Source: rs262298902
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107330032C>T

Allele/Variant
Source: rs236554476
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329457G>A

Allele/Variant
Source: rs579099280
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329625A>T

Allele/Variant
Source: rs213020582
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329434A>G

Allele/Variant
Source: rs582248361
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329532C>T

Allele/Variant
Source: rs246683927
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329984A>G

Allele/Variant
Source: rs246847037
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329408C>T

Allele/Variant
Source: rs30611320
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329980A>T

Allele/Variant
Source: rs235149004
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329834G>A

Allele/Variant
Source: rs223154812
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329932G>A